JPH08333270A - Cell activator - Google Patents
Cell activatorInfo
- Publication number
- JPH08333270A JPH08333270A JP7175340A JP17534095A JPH08333270A JP H08333270 A JPH08333270 A JP H08333270A JP 7175340 A JP7175340 A JP 7175340A JP 17534095 A JP17534095 A JP 17534095A JP H08333270 A JPH08333270 A JP H08333270A
- Authority
- JP
- Japan
- Prior art keywords
- extract
- cell
- skin
- trapa japonica
- activator
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
Landscapes
- Cosmetics (AREA)
- Medicines Containing Plant Substances (AREA)
Abstract
Description
【0001】[0001]
【産業上の利用分野】本発明は細胞賦活作用が高い化粧
品、食品或いは医薬品に関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to cosmetics, foods or pharmaceuticals having a high cell activating effect.
【0002】[0002]
【0003】菱実はヒシ科、ヒシ属のトラパ ナタンス
エル(Trapa natansL)と称し、通常ひ
しと呼ばれる植物の果実を乾燥したものである。ひしは
日本、朝鮮、中国の温帯から亜熱帯に分布し、池や沼に
はえる1年草で実は食用になる。従来の用途としては滋
養強壮、解熱剤として用いられる。さらに本発明者らに
よって、美白作用、ヒアルロニダーゼ活性阻害効果等が
あることを見いだされている。[0003] Hishomi is called Trapa natans L, which is a member of the family Rhizophora, and is a dried fruit of a plant usually called a rhombus. Hishi are distributed in temperate to subtropical regions of Japan, Korea, and China, and are annual edible plants that grow on ponds and swamps. As a conventional application, it is used as a nutritional tonic and antipyretic agent. Furthermore, the present inventors have found that they have a whitening effect, a hyaluronidase activity inhibitory effect, and the like.
【0004】[0004]
【発明が解決しようとする課題】本発明の目的は、皮膚
に適用して安全であると共に、皮膚を活性化させ、若々
しい肌を保つ細胞賦活剤を得ることである。SUMMARY OF THE INVENTION An object of the present invention is to obtain a cell activator which is safe when applied to the skin and which activates the skin and keeps youthful skin.
【0005】[0005]
【課題を解決する手段】本発明者らは、皮膚を活性化さ
せ、若々しい肌を保つ細胞賦活剤を得るため、食用にさ
れ、安全性が確認されている植物について効果を見たと
ころ、菱実の抽出物に非常に細胞賦活作用があることを
見いだした。菱実の利用方法としては、親水性有機溶媒
例えば、エタノール、メタノール、アセトン等で、或い
はこれらと水の混合溶媒で抽出する。しかしながら、化
粧品原料の抽出であるから、エタノール或いは水とエタ
ノールの混合溶媒での抽出が好ましいのは当然である。
また、場合によっては、グリセリン、1,3ブチレング
リコール、プロピレングリコール等の多価アルコール又
は多価アルコールと水の混液も抽出に利用できる。また
さらに凍結乾燥して粉体として利用することも利用方法
によっては有効である。Means for Solving the Problems The present inventors have found the effects on plants that are edible and have been confirmed to be safe in order to obtain a cell activator that activates the skin and maintains youthful skin. , Hishimi extract was found to have a very cell-activating effect. As a method for utilizing Hishimi, extraction is performed with a hydrophilic organic solvent such as ethanol, methanol, or acetone, or a mixed solvent of these and water. However, it is natural that extraction with ethanol or a mixed solvent of water and ethanol is preferable because it is extraction of cosmetic raw materials.
In some cases, a polyhydric alcohol such as glycerin, 1,3 butylene glycol, propylene glycol or the like or a mixed liquid of polyhydric alcohol and water can be used for extraction. Further, freeze-drying and using it as powder is also effective depending on the method of use.
【0006】この物質を他の化粧品原料例えばスクワラ
ン、ホホバ油等の液状油、ミツロウ、セチルアルコール
等の固体油、各種の活性剤、グリセリン、1,3ブチレ
ングリコール等の保湿剤や各種薬剤等を添加してさまざ
まな剤形の化粧料を調整することができる。例えばロー
ション、クリーム、乳液、パック等で目的に応じて利用
形態を考えればよい。[0006] This substance is used as other cosmetic raw materials, for example, liquid oils such as squalane and jojoba oil, solid oils such as beeswax and cetyl alcohol, various activators, moisturizing agents such as glycerin and 1,3 butylene glycol, and various agents. It can be added to adjust various dosage forms of cosmetics. For example, a lotion, a cream, a milky lotion, a pack, or the like may be used depending on the purpose.
【0007】[0007]
【製造例】以下に実際の抽出物の製造方法である製造例
を記載するが、本発明はこの製造例によって何ら限定さ
れるものではない。[Manufacturing Example] The following describes a manufacturing example which is a method for manufacturing an actual extract, but the present invention is not limited to this manufacturing example.
【0008】製造例 菱実の果実(乾燥品)を10gに50%エタノール水溶
液300mlを加えて時々攪拌しつつ5日間放置した。
これを濾過後凍結乾燥した。Production Example To 10 g of Hishimi fruit (dry product) was added 300 ml of a 50% ethanol aqueous solution, and the mixture was left for 5 days with occasional stirring.
This was filtered and freeze-dried.
【0009】 実施例−1 ローション オリーブ油 0.5 製造例の抽出物 0.5 ポリオキシエチレン(20E.O)ソルビタンモノステアレート 2.0 ポリオキシエチレン(60E.O)硬化ヒマシ油 2.0 エタノール 10.0 1.0%ヒアルロン酸ナトリウム水溶液 5.0 精製水 80.0Example-1 Lotion Olive oil 0.5 Extract of Production Example 0.5 Polyoxyethylene (20 EO) sorbitan monostearate 2.0 Polyoxyethylene (60 EO) hydrogenated castor oil 2.0 Ethanol 10.0 1.0% sodium hyaluronate aqueous solution 5.0 Purified water 80.0
【0010】 実施例−2 クリーム A スクワラン 20.5 オリーブ油 2.0 ミンク油 1.0 ホホバ油 5.0 ミツロウ 5.0 セトステアリルアルコール 2.0 グリセリンモノステアレート 1.0 ソルビタンモノステアレート 2.0 製造例の抽出物 0.5 B 精製水 47.9 ポリオキシエチレン(20E.O)ソルビタンモノステアレート 2.0 ポリオキシエチレン(60E.O)硬化ヒマシ油 1.0 グリセリン 5.0 1.0%ヒアルロン酸ナトリウム水溶液 5.0 パラオキシ安息香酸メチル 0.1 AとBをそれぞれ計量し、70℃まで加温し、BにAを
攪拌しつつ徐々に加えたのち、ゆっくり攪拌しつつ30
℃まで冷却した。Example-2 Cream A Squalane 20.5 Olive Oil 2.0 Mink Oil 1.0 Jojoba Oil 5.0 Beeswax 5.0 Cetostearyl Alcohol 2.0 Glycerin Monostearate 1.0 Sorbitan Monostearate 2. 0 Extract of Production Example 0.5 B Purified water 47.9 Polyoxyethylene (20 EO) sorbitan monostearate 2.0 Polyoxyethylene (60 EO) hydrogenated castor oil 1.0 Glycerin 5.0 1. 0% aqueous solution of sodium hyaluronate 5.0 Methyl paraoxybenzoate 0.1 A and B were weighed and heated to 70 ° C., A was slowly added to B while stirring, and then 30 while slowly stirring.
Cooled to ° C.
【0011】細胞賦活試験 1. 分植・作用 1)培養フラスコで培養した繊維芽細胞(大日本製薬/
セルシステムFb)をトリプシン−EDTA試薬(クラ
ボウ)にて剥離し、PBS(−)で細胞懸濁液を調整し
た(細胞濃度5x105cell/ml)。 2)24ウェルプレートに20%−FBS MEM 培
地と正常ヒト繊維芽細胞5000cell/well
分植し、CO2培養器で3日間培養した 3)培養液を除去し、無血清 MEM 培地に交換し、
さらに2日間培養した。 4) 無血清 MEM 培地で調整した検体溶液2ml
に交換し、10% FBS−MEM 培地 0.1ml
を添加(検体中の血清濃度0.5%)した。5日間培養
後、コラーゲン量及びミトコンドリア活性量の測定に供
した。なお、MEM 培地のみで培養したウェルをコン
トロールとした。Cell activation test 1. Splitting and action 1) Fibroblasts cultured in culture flask (Dainippon Pharmaceutical /
The cell system Fb) was stripped with a trypsin-EDTA reagent (Kurabo), and a cell suspension was adjusted with PBS (-) (cell concentration 5 × 10 5 cells / ml). 2) In a 24-well plate, 20% -FBS MEM medium and normal human fibroblasts 5000 cells / well
After planting and culturing in a CO2 incubator for 3 days, 3) remove the culture solution and replace with serum-free MEM
It was further cultured for 2 days. 4) 2 ml of sample solution prepared with serum-free MEM medium
To 10% FBS-MEM medium 0.1 ml
Was added (0.5% serum concentration in the sample). After culturing for 5 days, the amount of collagen and mitochondrial activity were measured. In addition, a well cultured only in MEM medium was used as a control.
【0012】2.ミトコンドリア活性測定法(MTT) 1)培養プレートより、検体1mlを抜き取り別のプレ
ートに移し、各ウェルの対照 とした。 2)MTT試薬0.1mlを各プレートに添加し4時間
インキュベートした。 3)0.01N HClを含む20%SDS試薬1ml
を加え一晩放置した。 4)570nmの吸光度を測定し、次式によりミトコン
ドリア活性(相対値)を求めた。 ミトコンドリア活性(単位細胞あたりの相対値)は次式
となる。 2. Mitochondrial activity measurement method (MTT) 1) 1 ml of a sample was withdrawn from the culture plate and transferred to another plate to serve as a control for each well. 2) 0.1 ml of MTT reagent was added to each plate and incubated for 4 hours. 3) 1 ml of 20% SDS reagent containing 0.01N HCl
Was added and left overnight. 4) The absorbance at 570 nm was measured, and the mitochondrial activity (relative value) was calculated by the following formula. The mitochondrial activity (relative value per unit cell) is given by the following formula.
【0013】[0013]
【表1】 なお、対照との相対値で表した。試験濃度は5ppmで
ある。[Table 1] The relative value with respect to the control was used. The test concentration is 5 ppm.
【0014】[0014]
【効果】このように、菱実の抽出物は、低濃度で、非常
に高い細胞賦活効果があり、皮膚を活性化させ、若々し
い肌を保つ作用がある細胞賦活剤を得た。[Effect] As described above, the Hishimi extract has a very high cell activating effect at a low concentration, and a cell activating agent having an action of activating the skin and maintaining youthful skin was obtained.
Claims (1)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP7175340A JPH08333270A (en) | 1995-06-06 | 1995-06-06 | Cell activator |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP7175340A JPH08333270A (en) | 1995-06-06 | 1995-06-06 | Cell activator |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH08333270A true JPH08333270A (en) | 1996-12-17 |
Family
ID=15994358
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP7175340A Pending JPH08333270A (en) | 1995-06-06 | 1995-06-06 | Cell activator |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH08333270A (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR100706282B1 (en) * | 2004-05-13 | 2007-04-11 | 학교법인 인제학원 | Composition comprising an extract of Trapa japonica Flerov. showing antioxidative effect |
KR101310655B1 (en) * | 2011-05-18 | 2013-09-24 | 엔프라니 주식회사 | Cosmetic composition which contains trapa japonica flerov. extraction as active compotnets and the preparation method thereof |
JP2014037399A (en) * | 2012-07-18 | 2014-02-27 | Up Well:Kk | Anti-glycation agent and method for producing the same |
JP2014094964A (en) * | 2008-08-29 | 2014-05-22 | Hayashikane Sangyo Kk | Maillard reaction inhibitor |
-
1995
- 1995-06-06 JP JP7175340A patent/JPH08333270A/en active Pending
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR100706282B1 (en) * | 2004-05-13 | 2007-04-11 | 학교법인 인제학원 | Composition comprising an extract of Trapa japonica Flerov. showing antioxidative effect |
JP2014094964A (en) * | 2008-08-29 | 2014-05-22 | Hayashikane Sangyo Kk | Maillard reaction inhibitor |
KR101310655B1 (en) * | 2011-05-18 | 2013-09-24 | 엔프라니 주식회사 | Cosmetic composition which contains trapa japonica flerov. extraction as active compotnets and the preparation method thereof |
JP2014037399A (en) * | 2012-07-18 | 2014-02-27 | Up Well:Kk | Anti-glycation agent and method for producing the same |
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